Basic info
Industry
medical equipment manufacturing
Sectors
Pharmaceutical
Artificial Intelligence
Regulatory Affairs
EU Legal Representative
European Union Authorised Representative
Person Responsible for Regulatory Compliance
Corrective and Preventive Action (CAPA)
Technical Files
Regulatory Strategy
Diagnostics
Digital Media
Internet of Medical Things
Medical Device
Software Validation
Machine Learning
IoMT
Risk Management
EU Person Responsible
Design Control
Cyber Security
Health Diagnostics
Health Care
Cyber security
Quality Management Systems
Clinical Evaluations
Quality Management
SaMD
Quality Compliance
Clinical Investigations
ISO 13485
Medical Devices
Digital Health
Design Files
EU Authorised Representative
Product Classification
Date founded
2019